Exciton-Phonon Interactions Govern Charge-Transfer-State Dynamics in CdSe/CdTe Two-Dimensional Colloidal Heterostructures

被引:33
|
作者
Pandya, Raj [1 ]
Chen, Richard Y. S. [1 ]
Cheminal, Alexandre [1 ]
Dufour, Marion [2 ]
Richter, Johannes M. [1 ]
Thomas, Tudor H. [1 ]
Ahmed, Shahab [3 ]
Sadhanala, Aditya [1 ]
Booker, Edward P. [1 ]
Divitini, Giorgio [4 ]
Deschler, Felix [1 ]
Greenham, Neil C. [1 ]
Ithurria, Sandrine [2 ]
Rao, Akshay [1 ]
机构
[1] Univ Cambridge, Cavendish Lab, JJ Thompson Ave, Cambridge CB3 OHE, England
[2] PSL Res Univ, CNRS, ESPCI Paris, LPEM, 10 Rue Vauquelin, F-75005 Paris, France
[3] Univ Cambridge, Inst Mfg, Dept Engn, 17 Charles Babbage Rd, Cambridge CB3 0FS, England
[4] Univ Cambridge, Dept Mat Sci & Met, 27 Charles Babbage Rd, Cambridge CB3 0FS, England
基金
英国工程与自然科学研究理事会;
关键词
TEMPERATURE-DEPENDENCE; QUANTUM-WELLS; CDSE NANOPLATELETS; RAMAN-SCATTERING; SEMICONDUCTOR NANOPLATELETS; URBACH TAIL; NANOCRYSTALS; CDTE; DOTS; PHOTOLUMINESCENCE;
D O I
10.1021/jacs.8b05842
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CdSe/CdTe core-crown type-II nanoplatelet heterostructures are two-dimensional semiconductors that have attracted interest for use in light-emitting technologies due to their ease of fabrication, outstanding emission yields, and tunable properties. Despite this, the exciton dynamics of these complex materials, and in particular how they are influenced by phonons, is not yet well understood. Here, we use a combination of femtosecond vibrational spectroscopy, temperature-resolved photoluminescence (PL), and temperature-dependent structural measurements to investigate CdSe/CdTe nanoplatelets with a thickness of four monolayers. We show that charge-transfer (CT) excitons across the CdSe/CdTe interface are formed on two distinct time scales: initially from an ultrafast (similar to 70 fs) electron transfer and then on longer time scales (similar to 5 ps) from the diffusion of domain excitons to the interface. We find that the CT excitons are influenced by an interfacial phonon mode at similar to 120 cm(-1), which localizes them to the interface. Using low-temperature PL spectroscopy we reveal that this same phonon mode is the dominant mechanism in broadening the CT PL. On cooling to 4 K, the total PL quantum yield reaches close to unity, with an,similar to 85% contribution from CT emission and the remainder from an emissive sub-band-gap state. At room temperature, incomplete diffusion of domain excitons to the interface and scattering between CT excitons and phonons limit the PL quantum yield to,similar to 50%. Our results provide a detailed picture of the nature of exciton-phonon interactions at the interfaces of 2D heterostructures and explain both the broad shape of the CT PL spectrum and the origin of PL quantum yield losses. Furthermore, they suggest that to maximize the PL quantum yield both improved engineering of the interfacial crystal structure and diffusion of domain excitons to the interface, e.g., by altering the relative core/crown size, are required.
引用
收藏
页码:14097 / 14111
页数:15
相关论文
共 50 条
  • [31] The thickness of the two-dimensional charge transfer state at the TTF-TCNQ interface
    Kattel, Bhupal
    Wang, Ti
    Kafle, Tika R.
    Chan, Wai-Lun
    ORGANIC ELECTRONICS, 2017, 48 : 371 - 376
  • [32] Influence of donor-to-acceptor ratio on excited-state electron transfer within covalently tethered CdSe/CdTe quantum dot colloidal heterostructures
    McGranahan, Caitlin R.
    Watson, David F.
    JOURNAL OF CHEMICAL PHYSICS, 2022, 156 (05):
  • [33] Exploring size and state dynamics in CdSe quantum dots using two-dimensional electronic spectroscopy
    Caram, Justin R.
    Zheng, Haibin
    Dahlberg, Peter D.
    Rolczynski, Brian S.
    Griffin, Graham B.
    Dolzhnikov, Dmitriy S.
    Talapin, Dmitri V.
    Engel, Gregory S.
    JOURNAL OF CHEMICAL PHYSICS, 2014, 140 (08):
  • [34] Ultrafast charge transfer dynamics pathways in two-dimensional MoS2-graphene heterostructures: a core-hole clock approach
    Garcia-Basabe, Yunier
    Rocha, Alexandre R.
    Vicentin, Flavio C.
    Villegas, Cesar E. P.
    Nascimento, Regiane
    Romani, Eric C.
    de Oliveira, Emerson C.
    Fechine, Guilhermino J. M.
    Li, Shisheng
    Eda, Goki
    Larrude, Dunieskys G.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (44) : 29954 - 29962
  • [35] Comment on "Evidence of many-particle interactions in two-dimensional charge-stabilized colloidal crystals"
    Reinke, D.
    PHYSICAL REVIEW LETTERS, 2006, 97 (11)
  • [36] Highly mobile charge-transfer excitons in two-dimensional WS2/tetracene heterostructures
    Zhu, Tong
    Yuan, Long
    Zhao, Yan
    Zhou, Mingwei
    Wan, Yan
    Mei, Jianguo
    Huang, Libai
    SCIENCE ADVANCES, 2018, 4 (01):
  • [37] Highly mobile charge-transfer excitons in two-dimensional tetracene-WS2 heterostructures
    Zhu, Tong
    Yuan, Long
    Zhao, Yan
    Zhou, Mingwei
    Wan, Yan
    Mei, Jianguo
    Huang, Libai
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [38] Excited state intramolecular charge transfer rates of p-dimethylaminobenzonitrile (DMABN) in solution: A two-dimensional dynamics perspective
    Kim, HJ
    Hynes, JT
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1997, 105 (2-3) : 337 - 343
  • [39] Two-dimensional femtosecond optical spectroscopy of trapping dynamics in a charge-transfer process
    Kess, Martin
    Engel, Volker
    CHEMICAL PHYSICS LETTERS, 2016, 650 : 41 - 46
  • [40] Enhancing Self-Trapped Exciton Emission via Energy Transfer in Two-Dimensional/Quantum Dot Perovskite Heterostructures
    Li, Wancai
    Hu, Long
    Ma, Jiaqi
    Jiang, Chuanxiu
    Zhang, Shuai
    Chen, Yingying
    Hu, Junchao
    Liu, Xinfeng
    Wu, Tom
    Li, Dehui
    ACS PHOTONICS, 2022, 9 (06) : 2008 - 2014